Variant report
Variant |
rs12720778 |
Chromosome Location |
chr2:21246207-21246208 |
allele |
C/T
|
Outlinks |
Ensembl
 
UCSC
|
rSNPs within LD-proxies of this variant (count:2)
Chromatin state (count:9 , 50 per page) page:
1
No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
1 |
chr2:21234800-21262200 |
Weak transcription |
Ovary |
ovary
|
2 |
chr2:21235000-21246600 |
Strong transcription |
Duodenum Mucosa |
Duodenum
|
3 |
chr2:21235000-21261800 |
Strong transcription |
Fetal Intestine Large |
intestine
|
4 |
chr2:21240000-21246600 |
Genic enhancers |
HepG2 |
liver
|
5 |
chr2:21240600-21250600 |
Weak transcription |
Adipose Nuclei |
Adipose
|
6 |
chr2:21242800-21251000 |
Weak transcription |
Left Ventricle |
heart
|
7 |
chr2:21246200-21247000 |
Weak transcription |
Fetal Intestine Small |
intestine
|
8 |
chr2:21246200-21247200 |
Strong transcription |
Liver |
Liver
|
9 |
chr2:21246200-21248400 |
Weak transcription |
Aorta |
Aorta
|
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